Pharmaceutical Online Videos

  1. PEI And Non-PEI Transfection Solutions For High Titers And Production 9/2/2025

    Discover optimized AAV production with polyethylenimine (PEI) and non-polyethylenimine transfection solutions that are designed to boost titers and streamline scalability.

  2. How CRISPR And LNP Accelerate Therapeutic Innovation Through Analytics 9/2/2025

    CRISPR gene editing and lipid nanoparticle delivery are revolutionizing precision medicine. Discover how optimized LNP systems and advanced analytics accelerate therapeutic development.

  3. What Is The Biggest Problem With Inspector Training And Qualification? 8/25/2025

    Discover how a truly blind system eliminates bias from the human inspection process, improving data accuracy and validation of automated inspection systems.

  4. Why Companies Should Record Training Data 8/25/2025

    Many companies don't formally track the training data from their new visual inspectors, missing out on valuable insights into their progress and readiness for qualification.

  5. Why Is The Identifier The Solution? 8/25/2025

    A biased inspection process can create a false baseline, negatively impacting the ability to accurately calibrate and validate automated inspection systems.

  6. Considerations For Single Use Disposables 8/21/2025

    In this segment from the Pharmaceutical Online Live event, “Contamination Control Strategies For Drug Manufacturers,” panelists talk about the pros and cons of using single use disposables, including the need for upstream controls. Not all single use disposable providers are created equal, and single use disposables may interact differently with products.  

  7. Importance Of Architectural Layout To Prevent Contamination 8/21/2025

    In this segment from the Pharmaceutical Online Live event, “Contamination Control Strategies For Drug Manufacturers,” panelists discuss the importance of unidirectional flow for preventing contamination, as well as specific architectural requirements related to the European Union's Annex 1 regulations. Poor or aging facility design is not an acceptable excuse for noncompliance.

  8. Mitigation Strategies For HVAC Recirculation 8/21/2025

    In this segment from the Pharmaceutical Online Live event, “Contamination Control Strategies For Drug Manufacturers,” panelists talk about three key aspects for maintaining clean air: pressurization (including the use of bubbles and sinks), process isolation, and segregation.

  9. Regulatory Guidance For Cleaning And Disinfecting 8/21/2025

    In this segment from the Pharmaceutical Online Live event, “Contamination Control Strategies For Drug Manufacturers,” panelists discuss evolving regulatory guidance for cleaning and disinfection, including revisions to PDA Technical Report 70 and USP 1072, and a new forthcoming technical report on material transfer.

  10. Understanding Barrier Systems 8/21/2025

    In this segment from the Pharmaceutical Online Live event, “Contamination Control Strategies For Drug Manufacturers,” panelists discuss fit-for-purpose barrier systems, including isolators, and the importance of understanding how to decontaminate barrier systems, perform aseptic operations, and considerations for open and closed RABs.